myelin-basic-protein and Spastic-Paraplegia--Hereditary

We describe the cases of two sisters with spastic paraplegia 11 (SPG11). The younger sister developed relapsing lesions in the brain white matter with enhancement during the acute phase that mimicked multiple sclerosis (MS). The elevation of myelin basic protein in the cerebrospinal fluid (CSF) suggested demyelination, but a normal IgG index, the absence of oligoclonal bands, and the ineffectiveness of steroid treatment indicate that an autoimmune mechanism may not have been involved. In these affected sisters, we identified novel compound heterozygous mutations in the SPG11 gene. Our cases indicate the possible existence of a broader phenotypic spectrum of SPG11 mutations.

Topics: Adolescent; Adult; Diagnosis, Differential; Female; Humans; Magnetic Resonance Imaging; Multiple Sclerosis; Mutation; Myelin Basic Protein; Pedigree; Proteins; Siblings; Spastic Paraplegia, Hereditary; White Matter; Young Adult